Literature DB >> 12611537

Photothermally induced Bergman cyclization of metalloenediynes via near-infrared ligand-to-metal charge-transfer excitation.

Brian J Kraft1, Nicole L Coalter, Mahendra Nath, Aurora E Clark, Allen R Siedle, John C Huffman, Jeffrey M Zaleski.   

Abstract

Reaction of 1,2-bis(tert-butyldimethylsilyloxy)-4,5-diiodobenzene with 2 equiv of phenylacetylene followed by deprotection with KF/HBr yields the catechol-enediyne ligand 4,5-bis(phenylethynyl)benzene-1,2-diol (CatED, 1). Metathesis of VO(SALIMH)ACAC.CH(3)OH (2) with 1 and subsequent air oxidation yields (4,5-bis(phenylethynyl)-1,2-dihydroxyphenyl)[4-(2-(salicylideneamino)ethyl)imidazolyl]oxovanadium(V).CH(3)OH [VO(SALIMH)CatED], (3), in 85%. The thermal Bergman cyclization temperature for 3 is very high (246 degrees C), which is expected for a rigid, benzannulated enediyne motif. The electronic spectrum of 3 exhibits two strong ligand-to-metal charge transfer (LMCT) transitions centered at 584 nm (epsilon = 6063 M(-)(1) cm(-)(1)) and 1028 nm (epsilon = 8098 M(-)(1) cm(-)(1)). These transitions derive from CatED-to-V(V) ligand-to-metal charge transfer, the assignment of which is verified by resonance enhancement of several CatED vibrational modes in the Raman spectra obtained with lambda = 785 vs lambda = 457.9 nm under low power and/or temperature conditions. At elevated temperatures (113-323 K) and powers (2-5 mW), excitation of 3 in the solid state with lambda = 785 nm leads to generation of a black, sparingly soluble, fluorescent product that exhibits weak vibrational features in the 580-600, 1200-1350, and 1450-1600 cm(-)(1) regions, indicative of V-O (CatED) and aromatic ring units. The C=C ring modes correspond well with the vibrational characteristics of poly(p-phenylene) and derivatives thereof. Additionally, materials generated in both the solid-state thermal and photothermal reactions of 3 demonstrate the formation of high molecular weight species ranging from 5000 to 274 000. On the basis of these data and the literature precedent for formation of poly(p-phenylene) via thermolysis of simple enediynes, the reaction poses a unique approach for photoinitiating Bergman cyclization with long-wavelength excitation, as well as the generation of polymeric products.

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Year:  2003        PMID: 12611537     DOI: 10.1021/ic0207045

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  6 in total

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3.  Designed metalloenediyne warheads damage DNA and outpace DNA polymerase.

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4.  Two-photon photochemical generation of reactive enediyne.

Authors:  Andrei Poloukhtine; Vladimir V Popik
Journal:  J Org Chem       Date:  2006-09-15       Impact factor: 4.354

5.  The Outliers: Metal-Mediated Radical Reagents for Biological Substrate Degradation.

Authors:  Meghan R Porter; Joan M Walker; Jeffrey M Zaleski
Journal:  Acc Chem Res       Date:  2019-06-25       Impact factor: 24.466

6.  Chelation-induced diradical formation as an approach to modulation of the amyloid-β aggregation pathway.

Authors:  Meghan R Porter; Akiko Kochi; Jonathan A Karty; Mi Hee Lim; Jeffrey M Zaleski
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  6 in total

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